NDC product
Multi-Phenolic
NDC 44911-0649 · Energique, Inc.
Key facts
| Product NDC | 44911-0649 |
|---|---|
| Proprietary name | Multi-Phenolic |
| Nonproprietary name | Mannose, 5-Hydroxytryptophan, Acetaldehyde, Acetylcholine Chloride, Ascorbicum Acidum, Aspartame, Butylated Hydroxytoluene, Caffeic Acid, Candida Albicans, Cinnamic Acid, Coniferyl Alcohol, Coumarinum and 18 more |
| Substances | MANNOSE, D-, OXITRIPTAN, ACETALDEHYDE, ACETYLCHOLINE CHLORIDE, ASCORBIC ACID, ASPARTAME, BUTYLATED HYDROXYTOLUENE, CAFFEIC ACID, CANDIDA ALBICANS, CINNAMIC ACID, CONIFERYL ALCOHOL, COUMARIN and 25 more |
| Dosage form | LIQUID |
| Route | ORAL |
| Labeler | Energique, Inc. |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Allergens [CS], Amino Acids, Aromatic [CS], Aromatic Amino Acid [EPC], Ascorbic Acid [CS], Catecholamine [EPC] and 16 more |
| Marketing start | Jan 11, 2022 |
| Listing certified through | Dec 31, 2026 |
At a glance
- 1–9 Package NDCs
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About National Drug Codes (NDC)
The National Drug Code (NDC) is the FDA's product identifier for drugs; the product NDC identifies the labeler and product, and each package adds a package code.
Source: U.S. Food and Drug Administration (FDA), National Drug Code Directory · Source date: